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DOXEPIN HYDROCHLORIDE

NDC 46708-640 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA215076
Dosage form / routeCAPSULE · ORAL
Active ingredientsDOXEPIN HYDROCHLORIDE (100 mg/1)
Marketing started20210423
Package count2

External sources

Source: openFDA. Public-domain (CC0).